Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study

dc.contributor.author
Wagstyl, Konrad
dc.contributor.author
Whitaker, Kirstie
dc.contributor.author
Raznahan, Armin
dc.contributor.author
Seidlitz, Jakob
dc.contributor.author
Vértes, Petra E
dc.contributor.author
Foldes, Stephen
dc.contributor.author
Humphreys, Zachary
dc.contributor.author
Hu, Wenhan
dc.contributor.author
Mo, Jiajie
dc.contributor.author
Likeman, Marcus
dc.contributor.author
Davies, Shirin
dc.contributor.author
Lenge, Matteo
dc.contributor.author
Cohen, Nathan T
dc.contributor.author
Tang, Yingying
dc.contributor.author
Wang, Shan
dc.contributor.author
Ripart, Mathilde
dc.contributor.author
Chari, Aswin
dc.contributor.author
Tisdall, Martin
dc.contributor.author
Bargalló Alabart, Núria
dc.contributor.author
Conde Blanco, Estefanía
dc.contributor.author
Pariente, Jose Carlos
dc.contributor.author
Pascual-Diaz, Saül
dc.contributor.author
Delgado-Martínez, Ignacio
dc.contributor.author
Pérez-Enríquez, Carmen
dc.contributor.author
Lagorio, Ilaria
dc.contributor.author
Abela, Eugenio
dc.contributor.author
Mullatti, Nandini
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O'Muircheartaigh, Jonathan
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Vecchiato, Katy
dc.contributor.author
Liu, Yawu
dc.contributor.author
Caligiuri, Maria
dc.contributor.author
Sinclair, Ben
dc.contributor.author
Vivash, Lucy
dc.contributor.author
Willard, Anna
dc.contributor.author
Kandasamy, Jothy
dc.contributor.author
McLellan, Ailsa
dc.contributor.author
Sokol, Drahoslav
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Semmelroch, Mira
dc.contributor.author
Kloster, Ane
dc.contributor.author
Opheim, Giske
dc.contributor.author
Yasuda, Clarissa
dc.contributor.author
Zhang, Kai
dc.contributor.author
Hamandi, Khalid
dc.contributor.author
Barba, Carmen
dc.contributor.author
Guerrini, Renzo
dc.contributor.author
Gaillard, William Davis
dc.contributor.author
You, Xiaozhen
dc.contributor.author
Wang, Irene
dc.contributor.author
González Ortiz, Sofía
dc.contributor.author
Severino, Mariasavina
dc.contributor.author
Striano, Pasquale
dc.contributor.author
Tortora, Domenico
dc.contributor.author
Kalviainen, Reetta
dc.contributor.author
Gambardella, Antonio
dc.contributor.author
Labate, Angelo
dc.contributor.author
Desmond, Patricia
dc.contributor.author
Lui. Elaine
dc.contributor.author
O'Brien, Terry
dc.contributor.author
Shetty, Jay
dc.contributor.author
Jackson, Graeme
dc.contributor.author
Duncan, John S
dc.contributor.author
Winston, Gavin P
dc.contributor.author
Pinborg, Lars
dc.contributor.author
Cendes, Fernando
dc.contributor.author
Cross, Judith Helen
dc.contributor.author
Baldeweg, Torsten
dc.contributor.author
Adler, Sophie
dc.date.issued
2026-01-26T09:51:09Z
dc.date.issued
2026-01-26T09:51:09Z
dc.date.issued
2021-11-29
dc.date.issued
2026-01-26T09:51:09Z
dc.identifier
2470-9239
dc.identifier
https://hdl.handle.net/2445/226125
dc.identifier
756753
dc.identifier
34845719
dc.description.abstract
Objective: Drug-resistant focal epilepsy is often caused by focal cortical dysplasias (FCDs). The distribution of these lesions across the cerebral cortex and the impact of lesion location on clinical presentation and surgical outcome are largely unknown. We created a neuroimaging cohort of patients with individually mapped FCDs to determine factors associated with lesion location and predictors of postsurgical outcome. Methods: The MELD (Multi-centre Epilepsy Lesion Detection) project collated a retrospective cohort of 580 patients with epilepsy attributed to FCD from 20 epilepsy centers worldwide. Magnetic resonance imaging-based maps of individual FCDs with accompanying demographic, clinical, and surgical information were collected. We mapped the distribution of FCDs, examined for associations between clinical factors and lesion location, and developed a predictive model of postsurgical seizure freedom. Results: FCDs were nonuniformly distributed, concentrating in the superior frontal sulcus, frontal pole, and temporal pole. Epilepsy onset was typically before the age of 10 years. Earlier epilepsy onset was associated with lesions in primary sensory areas, whereas later epilepsy onset was associated with lesions in association cortices. Lesions in temporal and occipital lobes tended to be larger than frontal lobe lesions. Seizure freedom rates varied with FCD location, from around 30% in visual, motor, and premotor areas to 75% in superior temporal and frontal gyri. The predictive model of postsurgical seizure freedom had a positive predictive value of 70% and negative predictive value of 61%. Significance: FCD location is an important determinant of its size, the age at epilepsy onset, and the likelihood of seizure freedom postsurgery. Our atlas of lesion locations can be used to guide the radiological search for subtle lesions in individual patients. Our atlas of regional seizure freedom rates and associated predictive model can be used to estimate individual likelihoods of postsurgical seizure freedom. Data-driven atlases and predictive models are essential for evidence-based, precision medicine and risk counseling in epilepsy.
dc.format
14 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
John Wiley & Sons
dc.relation
Reproducció del document publicat a: https://doi.org/10.1111/epi.17130
dc.relation
Epilepsia Open, 2021, vol. 63, num.1, p. 61-74
dc.relation
https://doi.org/10.1111/epi.17130
dc.rights
cc-by-nc-nd (c) Wagstyl K et al., 2021
dc.rights
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Neurocirurgia
dc.subject
Epilèpsia
dc.subject
Neurosurgery
dc.subject
Epilepsy
dc.title
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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